ライフサイエンスコーパス: be stimulated with

1 EC) grown on laminar-flow perfusion channels were stimulated with 1 mug/mL lipopolysaccharide for 6 h

2 Human periodontal ligament (PDL) cells were stimulated with: 1) 10 ng/mL BMP2; 2) 1 mug/mL doxy

3 When macrophages were stimulated with 10 isolates of each RST1, RST2, or

4 r chondrocytes isolated from ankle cartilage were stimulated with 10 ng/ml of interleukin-1beta (IL-1

5 d when unstimulated; however, when the cells were stimulated with 10 nm alpha-thrombin, we were able

6 ed CD69 expression of gammadeltaT cells that were stimulated with 100 ng/mL lipopolysaccharide.

7 Isolated peripheral blood neutrophils were stimulated with 19 periodontal bacteria.

8 nonuclear cells from 45 children with asthma were stimulated with 2 and 200 ng/ml lipopolysaccharide

9 When cnrN cells expressing myc-tagged CnrN are stimulated with a mixture of rAprA and rCfaD, levels

10 ing reminiscent of wakefulness when cultures are stimulated with a mixture of waking neurotransmitter

11 The retina was stimulated with a liquid crystal display (LCD) integ

12 Each eye was stimulated with a low (Lc) and a high (Hc) Michelson

13 When PBMCs from patients with Lyme arthritis were stimulated with a B burgdorferi RST1 strain, the 18

14 11 engagement, human RA synovial fibroblasts were stimulated with a chimeric construct consisting of

15 T cells that were stimulated with a high concentration of antigen upr

16 sing the protective HLA-DQB1*06 (DQ6) allele were stimulated with a mixture of streptococcal superant

17 Cells were stimulated with a monoclonal antibody against CD3,

18 CD4 T cells were stimulated with Ag presented by B7-negative APC and

19 Notably, when the iTreg were stimulated with Ag, treatment with IL-2/anti-IL-2 c

20 hmatic and non-atopic non-asthmatic subjects were stimulated with agonists to TLR3, TLR4 & TLRs7-9 an

21 Cells were stimulated with agonists, and secretion of Hsp90, u

22 m the All Babies In Southeast Sweden cohort, were stimulated with Ags (tetanus toxoid and beta-lactog

23 eosinophils were incubated with T cells that were stimulated with allogeneic leukocytes or CD3/CD28 c

24 s if, in parallel to antigen uptake, the DCs were stimulated with alpha-CD40.

25 These cars are designed to be stimulated with an electric field gradient from a sca

26 ng slow waves was modified if the animal had been stimulated with an odor within the receptive field

27 AF was stimulated with an intra-esophageal burst pacing pro

28 lar neurons predicted which of four pathways were stimulated with an accuracy of 76% and performed si

29 PBMCs were stimulated with an anti-CD3 antibody and IL-4 or IL

30 Primary cultures of hfRPE were stimulated with an inflammatory cytokine mixture (I

31 PBMCs were stimulated with and without CpG and were subsequent

32 However, when ECs are stimulated with Ang1 and Ang2, Ang2 dose-dependently

33 Cardiomyocyte hypertrophy was stimulated with AngII or vasopressin, significantly

34 of post-acute kidney injury (post-AKI) rats were stimulated with angiotensin II and elevated Na+ (10

35 crovascular endothelial cells (MPMVECs) that were stimulated with angiotensin II; the interaction of

36 blood mononuclear cells from healthy donors were stimulated with anti-CD3 and anti-CD28 beads, and t

37 T cells were stimulated with anti-CD3 in the absence or presence

38 hy donor peripheral blood-derived Tregs that were stimulated with anti-CD3/CD28 monoclonal antibodies

39 Purified naive CD4+ T cells were stimulated with anti-CD3/CD28 under Th1, Th2, Th17,

40 Isolated B cells were stimulated with anti-cluster of differentiation (CD

41 Human peripheral blood-derived mast cells were stimulated with anti-IgE Ab in the presence of dexa

42 Human B cells were stimulated with anti-IgM antibody, and effects of I

43 M detected no ZAP70 recruitment when T cells were stimulated with antigen in the presence of the src-

44 moted disinhibited neurite growth when cells were stimulated with appropriate neurotrophic factors.

45 released from platelets whose NO production was stimulated with ATP (a nitric oxide synthase stimulu

46 m donors sensitized to grass or birch pollen were stimulated with autologous allergen-pulsed dendriti

47 Enriched NK cells were stimulated with autologous iCD4 cells or with uninf

48 CD4(+) T cells from allergic donors were stimulated with autologous monocyte-derived allerge

49 ed from 14-week-old but not younger NOD mice were stimulated with both p217 and p290.

50 In total, 40 clones were stimulated with both PPD and PPD-modified HSA.

51 atients (n=24) and healthy volunteers (n=30) were stimulated with both unspecific and pathogen-specif

52 portion of transient fusions when astrocytes were stimulated with bradykinin, a stimulus otherwise re

53 n peripheral blood mononuclear cells (PBMCs) were stimulated with C. burnetii Nine Mile and the Dutch

54 Normal esophageal keratinocytes were stimulated with calcium chloride to induce terminal

55 Peripheral blood mononuclear cells were stimulated with Candida albicans.

56 Fresh mouse and human eosinophils were stimulated with CCL11 and CCL24, and the secretion

57 In vitro, cultured HSCs were stimulated with cholangiocyte supernatants and alph

58 MECs were stimulated with cholinergic and alpha(1)-adrenergic

59 from 28 RA patients and 18 healthy controls were stimulated with citrullinated or noncitrullinated a

60 T-cell interferon gamma (IFNgamma) secretion was stimulated with CMV lysate.

61 after (POST) 30-minutes of cycling exercise were stimulated with CMV (pp65 and IE1) and EBV (LMP2A a

62 CFSE-labeled PBMCs were stimulated with CMV, tetanus toxoid (TT), and C alb

63 ation, as it proceeds even when the receptor is stimulated with collagenase-resistant collagen I (r/r

64 hesis, cultured respiratory epithelial cells were stimulated with combinations of purified siderophor

65 Normal human bronchial epithelials were stimulated with conditioned medium from monocytes i

66 Human lung fibroblasts grown in collagen were stimulated with conditioned medium from Mtb-infecte

67 nt, where it remains until the corticotropes are stimulated with corticotropin releasing factor (CRF)

68 Cultured hRPE and mRPE cells were stimulated with cytokines for various times or with

69 When LPS-primed glial cells were stimulated with DAMPs under acidic conditions (pH 6

70 ulosis-induced production of cytokines, PBMC were stimulated with DEP and M. tuberculosis or purified

71 ated from peripheral blood of healthy donors were stimulated with different combinations of molecules

72 Air-liquid interface cultures were stimulated with different concentrations of JNJ-264

73 RASFs were stimulated with different concentrations of visfati

74 The model was stimulated with dopamine pulses mimicking those reco

75 Human PDL cells and primary osteoblasts were stimulated with doses of 1 to 200 ng/mL BMP2.

76 , peripheral blood mononuclear cells (PBMCs) were stimulated with each of the VLPs, and secretion of

77 lating proteasomal proteolysis in cells that are stimulated with EGF.

78 The cells were stimulated with EGF (10(-7) M) for 1 and 5 minutes

79 The cells were stimulated with EGF (10(-7) M) for 1 minute to 24 h

80 Rabbit corneal epithelial (RCE) cells were stimulated with EGF or LXA4 at different times.

81 d phosphorylation, only those receptors that were stimulated with EGF progressed to lysosomal degrada

82 on (20 s) to a complex moving pattern, while being stimulated with either sham or tRNS across differe

83 shwork (TM) cells and corneoscleral explants were stimulated with either dexamethasone (DEX) or trans

84 HLA-B8(+) HLA-B44(-) EBV-seropositive PBMCs were stimulated with either HLA-B*44:02(+) or HLA-B*44:0

85 g age-matched male control subjects (n = 16) were stimulated with either lipopolysaccharide or phytoh

86 Vascular smooth muscle cells were stimulated with either SAA or CRP (1 to 100 mg/L) a

87 enic T cells isolated from Mus musculus that were stimulated with either T-cell receptor (TCR) cross-

88 r during the pollen season or out of season, were stimulated with either TG extract or a pool of prev

89 ain surgery, specific areas in the brain can be stimulated with electrical impulses to reversibly cha

90 Nerves were stimulated with electrical field stimulation (0.1-2

91 ro model, primary smooth muscle cells (SMCs) were stimulated with elevated transforming growth factor

92 eration was significantly elevated when PMNs were stimulated with EMD (200 mug/mL) (P <0.01).

93 of runx2 and desmin, and the cocultures that were stimulated with EMD and BMP-2 achieved significantl

94 Human PDL cells were stimulated with EMD.

95 NRVMs with PLCepsilon depletion were stimulated with endothelin (ET-1), norepinephrine,

96 hin non-gas-permeable microchannels, as they are stimulated with endotoxin.

97 elial cells and glomerular endothelial cells were stimulated with endotoxins, cytokines, and human le

98 red primary oligodendroglial precursor cells were stimulated with ENV protein to determine the effect

99 Human mast cells were stimulated with epithelial cell-derived supernatant

100 Cells were stimulated with equimolar amounts of rFlaA, rBet v

101 Whole blood was stimulated with Escherichia coli derived lipopolysac

102 nts expressing wild-type or polymorphic TLR4 were stimulated with Escherichia coli (predominantly hex

103 er RNAs is enriched when breast cancer cells are stimulated with estrogen.

104 tive to normal cells, even when normal cells are stimulated with exogenous epidermal growth factor.

105 e cooperativity, and its autoproteolysis can be stimulated with exogenous substrates or peptides that

106 Neurons were stimulated with flickering, full-field luminance no

107 Antennae were stimulated with forces approximating those of natur

108 response was detected when Gr64 mutant flies were stimulated with fructose.

109 Moreover, TEC were stimulated with genomic double-stranded (ds)DNA or

110 MIN6 beta cells and mouse islets were stimulated with globular (2.5 mug/ml) or full-lengt

111 This DC subset was stimulated with granulocyte-macrophage colony-stimul

112 2) or variant TLR2 genes (HEK293-TLR2-R753Q) were stimulated with HCV core and NS3 proteins.

113 ells (PBMC) from 20 HDM-allergic individuals were stimulated with HDM extracts and assayed with a set

114 ells (PBMC) from 20 HDM-allergic individuals were stimulated with HDM extracts and assayed with a set

115 HDM allergic and 10 non-allergic individuals were stimulated with HDM extracts and assayed with a set

116 ungal host defense against C. albicans PBMCs were stimulated with heat-killed (HK) C. albicans in the

117 Macrophages and PMNs of BHS and DS were stimulated with heat-killed M. haemolytica or LPS.

118 Human corneal epithelial (HCE) cells were stimulated with HGF with or without bpV(phen).

119 signaling in a coordinated manner when cells are stimulated with high levels of TGF-beta.

120 plasma levels, PBMCs from uninfected donors were stimulated with HIV-1 infectious virions, HIV-1 ssR

121 rimary human aortic endothelial cells (HAEC) were stimulated with HLA class I antibodies in the prese

122 16HBE cells were stimulated with house dust mite (HDM) extracts.

123 Caco-2 monolayers were stimulated with human IgE-antigen (Ag) complexes.

124 First, "donor"-derived CD8 T cells were stimulated with human leukocyte antigen-unmatched "

125 uccinimidyl ester-labeled human CD4+ T cells were stimulated with human or pig PBMC.

126 Active adenosine release was stimulated with hypoxia and trains of electrical sti

127 Bone marrow-derived myeloid DCs were stimulated with ICs composed of IgG autoantibody an

128 ription factor STAT2 only in cells that have been stimulated with IFN-I.

129 IOBA-NHC and Jurkat cells were stimulated with IFNgamma, TNFalpha, alphaFas, or PM

130 Both cell types were stimulated with IgE-ICs consisting of 4-hydroxy-3-i

131 MCF-7 cells were stimulated with IGF-I for 3 or 24 hours and were pr

132 Primary KCs were stimulated with IL-17 or TNF-alpha alone, or in com

133 Primary bronchial epithelial cells were stimulated with IL-17A and/or IL-22, with and witho

134 with no evidence of translation unless cells were stimulated with IL-1alpha.

135 Therefore, normal tendon explants were stimulated with IL-1beta and prostaglandin E2, and

136 Astrocytes were stimulated with IL-1beta or TNF-alpha, and CCL2 and

137 pression was detected only when tendon cells were stimulated with IL-1beta, and CTGF and significantl

138 L-5 and IL-13 expression by human ILC2s that were stimulated with IL-2 and IL-33.

139 al cells from healthy and asthmatic subjects were stimulated with IL-22, IFN-gamma, or the combinatio

140 In contrast, when basophils were stimulated with IL-3, loss of STIM2, but not STIM1,

141 o the generation of IgE, naive human B-cells were stimulated with IL-4 and anti-CD40.

142 When intestinal organoids were stimulated with IL-4, tuft cells and IL-25 were ind

143 , and IL-22 were blocked when naive Th cells were stimulated with IL-6 and IL-23.

144 However, it did not do so when ILC2s were stimulated with IL-7 and thymic stromal lymphopoiet

145 the vagus nerve to spleen circuit, which has been stimulated with implantable devices to improve auto

146 Fetal cardiovascular function was stimulated with increasing bolus doses of phenylephr

147 he human HSC line LX2 and primary human HSCs were stimulated with increasing doses of IL-17A and comp

148 In contrast, cyanobacteria were stimulated with increasing Fe concentration.

149 DCs were stimulated with influenza-J-LEAPS peptides (influen

150 sing the human insulin receptor and rat IRS1 were stimulated with insulin in the absence or presence

151 When cells were stimulated with insulin-like growth factor-1 (IGF-1

152 lower than those observed when CD14(+) cells were stimulated with interferon.

153 eron (IFN-gamma)-producing NK cells that had been stimulated with interleukin-12 (IL-12)/IL-15.

154 expression in vitro, normal tendon explants were stimulated with interleukin-1 beta and prostaglandi

155 Chondrocytes were stimulated with interleukin-1beta (IL-1beta) in vit

156 rt hairpin RNA to suppress FSTL1 expression, were stimulated with interleukin-1beta (IL-1beta), tumor

157 (PBMC), CD4+ T cells, or CD4+ CD25- T cells were stimulated with irradiated human or wild type (WT)

158 hydrochloride (ISO; 30 minutes) pretreatment were stimulated with ISO (10 minutes).

159 circumvallate taste buds and the taste buds were stimulated with KCl (50 mm) or a mixture of taste c

160 nd primary human bronchial epithelial cells, were stimulated with LIGHT and LTalphabeta, and expressi

161 Cord blood was stimulated with lipid A, peptidoglycan (Ppg), or PHA

162 nt macrophages when the cells had previously been stimulated with lipopolysaccharide (LPS) or E. coli

163 Bone marrow-derived macrophages (BMMs) were stimulated with lipopolysaccharide (LPS) and were e

164 ures of mononuclear cells from patients that were stimulated with lipopolysaccharide, with or without

165 Cells were stimulated with live or sonicated B. burgdorferi or

166 When monocytes were stimulated with live P. acnes, caspase-1 and caspas

167 Human corneal epithelial cells (HCECs) were stimulated with LL-37.

168 Aortic EC were stimulated with low-dose TNFalpha (0.3 ng/ml) in a

169 uced in these macrophages and MoDM when they are stimulated with LPS.

170 sa infection when the animals had previously been stimulated with LPS.

171 cells were treated with TE 90 minutes before being stimulated with LPS (TE90 DCs).

172 y, decidual DCs remained immobile even after being stimulated with LPS and exhibiting responsiveness

173 acrophages were treated with collinin before being stimulated with LPS.

174 Venous blood from human volunteers was stimulated with LPS, MPLA or vehicle.

175 ed with decreased NO production by PECs that were stimulated with LPS and gamma interferon in the pre

176 When rat macrophages were stimulated with LPS and IFN-gamma separately, SP-A

177 Monocytes and T lymphocytes were stimulated with LPS and PHA, respectively.

178 hages (Mphi) and PMN from BALB/c and B6 mice were stimulated with LPS and treated with rVIP.

179 type 2 cytokine gene expression, macrophages were stimulated with LPS, and the expression of IL-4 and

180 Primary mouse macrophages were stimulated with LPS/IFNgamma or IL4 with or without

181 Respiratory afferents have been stimulated with mechanical loads applied to breathi

182 rom peripheral blood and intestinal biopsies were stimulated with microbial phosphoantigen (1-hydroxy

183 te and shed active matriptase when the cells are stimulated with mildly acidic buffer or the hypoxia-

184 Human leukocytes were stimulated with mitogens on board the International

185 uman oligodendrocytes precursor cells (OPCs) were stimulated with moderate intensity SMF (0.3 T) for

186 s with TB or defective IFN-gamma receptor 1* were stimulated with Mtb antigen and SLPI, and IFN-gamma

187 Murine or human macrophages were stimulated with native fibrinogen (nFb), cFb, or in

188 DCs were stimulated with nCup a 1 and tested for their biolo

189 CD34(+) cells and HRECs were stimulated with NGF (1 to 4 pM) for 24, 48, and 72

190 RAW 264.7 macrophages or Kupffer cells were stimulated with oleate or palmitate, and levels of

191 Hsp90 release was stimulated with optimal doses of estradiol, IL-1, an

192 Human primary T cells were stimulated with or without anti-CD3 plus anti-CD28

193 The fibroblasts were stimulated with or without transforming growth fact

194 eatment in period 2; and hepatic lipogenesis was stimulated with oral fructose administration.

195 hatase positive colony size in cultures that were stimulated with osteoblast differentiation media.

196 also prevented activation of ERK1/2 when ECs were stimulated with other pro-angiogenic growth factors

197 PBMCs from 80 peanut-allergic patients were stimulated with overlapping 20-mer Ara h 2 peptides

198 ls from HIV-1-seropositive (HIV(+)) subjects were stimulated with overlapping RT peptide pools.

199 itope mapping, Mal d 1-specific T-cell lines were stimulated with overlapping synthetic 12-mer peptid

200 Human CAECs were stimulated with oxLDL.

201 Peripheral blood mononuclear cells were stimulated with P. falciparum antigen, and interfer

202 and TLR4, HGF and HPDLF from the same donors were stimulated with P. gingivalis LPS or with two synth

203 rom 3-day-old NZO and control C57BL/6J mice, were stimulated with P. gingivalis.

204 endritic cells (mdDC) from allergic patients were stimulated with Pam3CSK4 (TLR1/2 ligand), FSL-1 (TL

205 n a realistic 3D immersive environment while being stimulated with particular tCS patterns.

206 nsiveness was characterized, BAL macrophages were stimulated with pathogenic versus commensal microor

207 THP-1 cells were stimulated with Pg-DNA (100 ng/muL), Fn-DNA (100 ng

208 man mandibular osteoblast-like cells (HMOBs) were stimulated with PGE2.

209 gation and puncture, thoracic aorta segments were stimulated with phenylephrine in the presence or ab

210 Cells were stimulated with phorbol ester and ionomycin in the

211 After cells were stimulated with phorbol myristate acetate, the amou

212 When human aortic endothelial cells were stimulated with physiologic concentrations of fruct

213 inhibited motility of MCF-10A cells that had been stimulated with PKC activator diacylglycerol lacton

214 ed human HSC line hTERT and primary rat HSCs were stimulated with platelet-derived growth factor (PDG

215 When NIH 3T3 cells were stimulated with platelet-derived growth factor to g

216 fness responses are most robust when T cells are stimulated with pMHC rather than anti-CD3epsilon, co

217 Monocyte-derived dendritic cells (DCs) were stimulated with pneumococcal peptidoglycan (PGN) in

218 d peripheral blood mononuclear cells (PBMCs) were stimulated with poliovirus vaccine, and memory T ce

219 HPDLSCs were stimulated with Poly I:C (0.0001-1 ug/mL), Pam3CSK4

220 Fibroblast-like synoviocytes were stimulated with polyinosinic-polycytidylic acid (po

221 ed silencing of MyD88 or TRAM, HGF and HPDLF were stimulated with Porphyromonas gingivalis (Pg) lipop

222 atients, but not tolerant/naive individuals, were stimulated with PPD and PPD-modified HSA.

223 retreatment with single triterpenoids, cells were stimulated with pro-inflammatory cytokines (TNF-alp

224 BBE, HT29-Cl.19A, and human T cells (Jurkat) were stimulated with pro-inflammatory cytokines in the p

225 Fibroblasts were stimulated with proinflammatory cytokines (tumor ne

226 The cells were stimulated with PTH or PGE2 to induce MMP-13 mRNA e

227 HCAECs were stimulated with purified Aa serotype b lipopolysacc

228 When bone marrow cells derived from Xid mice were stimulated with receptor activator of NF-kappaB lig

229 m injured explants, rested explants that had been stimulated with recombinant FGF-2 or FGF-18, or who

230 BALB/c mice (peritoneal/bone marrow derived) were stimulated with recombinant a2NTD in both ex vivo a

231 Purified eosinophils were stimulated with recombinant human TSLP.

232 ultures of human gingival fibroblasts (HGFs) were stimulated with recombinant TGF-beta1 and TNF-alpha

233 Primary endothelial cells were stimulated with recombinant VEGF and exposed to hyp

234 Parallel samples were stimulated with related nonsteroidal anti-inflammat

235 d mononuclear cells (PBMC) from these groups were stimulated with relevant antigen for 48 h and flow

236 Isolated human CD3+T cells were stimulated with RNase 7 and screened for possible e

237 nterfering RNA-induced downregulation of MD2 were stimulated with RWPE, other pollen allergic extract

238 In addition, when ECs were stimulated with s-FKN, greater adhesion of human ne

239 of school-age children, whole-blood cultures were stimulated with S. mansoni soluble egg antigen (SEA

240 type and TLR2, TLR4, and MyD88 knockout mice were stimulated with Salmonella vector BRD509, the SBR-e

241 When DCs were stimulated with serotype b of A. actinomycetemcomit

242 tivating p21 expression when quiescent cells are stimulated with serum to reenter the cell cycle.

243 ON and OFF ganglion cells were stimulated with similar efficacy.

244 Peripheral blood mononuclear cells (PBMC) were stimulated with SLA to determine the frequencies of

245 lenocytes from wild-type or LAIR-1(-/-) mice were stimulated with soluble anti-CD3 Ab in the presence

246 y donors and/or respiratory epithelial cells were stimulated with soluble antigens or inactivated int

247 n PBMC and purified naive and memory B cells were stimulated with specific ligands for TLR2, TLR3, TL

248 Bovine articular chondrocytes were stimulated with sphingomyelinase (SMase) to increas

249 Endothelial cells were stimulated with sphingosine 1-phosphate receptor 1

250 e TOFs, specific regions of the rod OS could be stimulated with spots of light highly confined in spa

251 Peripheral blood mononuclear cells were stimulated with Staphylococcus aureus and Mycobacte

252 human cord blood-derived cultured mast cells were stimulated with substance P (SP) or IgE/anti-IgE wi

253 type, trypsinogen 7, or cathepsin B-deleted) were stimulated with supramaximal cerulein, and the cyto

254 In vivo-primed T cells were stimulated with syngeneic APCs, with or without the

255 s the major promoter used when human T cells were stimulated with TGF-beta1 and fibroblast growth fac

256 l interference RNA (siRNA)-transfected NHLFs were stimulated with TGF-beta1.

257 Human primary lung fibroblasts were stimulated with TGFbeta or IGFBP-3 in the presence

258 d peripheral blood mononuclear cells (PBMCs) were stimulated with TGFbeta, IL-13, poly(I-C), or TSLP.

259 porate an oxygen-diffusion gradient and that are stimulated with the neurotransmitter noradrenaline m

260 d after overnight starvation, expanded cells are stimulated with the same peptides from the initial c

261 Whole blood was stimulated with the M. tuberculosis-specific antigen

262 Cells were stimulated with the aromatase substrate, androstene

263 the angiotensin II type 1A receptor (AT1aR) were stimulated with the beta-arrestin-biased ligand Sar

264 t of these signaling events when eosinophils were stimulated with the combination of TNF-alpha plus I

265 e between sample treatment groups, microglia were stimulated with the endotoxin lipopolysaccharide (L

266 Acini were stimulated with the P2X(7) receptor agonist, (benzo

267 Acini were stimulated with the P2X7 receptor agonist, (benzoyl

268 Extracted monocytes were stimulated with the toll-like receptor (TLR)-4 liga

269 Bim(-/-) mice were stimulated with thioglycollate or LPS and examined

270 hRPE cells were stimulated with thrombin TNF-alpha, monocytes, and

271 When washed human platelets were stimulated with thrombin, cAMP-dependent phosphodie

272 ys, non-transfected MDCK-II and HEK293 cells were stimulated with thrombin.

273 e phosphorylated in kindlin-3 when platelets were stimulated with thrombin.

274 When HEL cells were stimulated with thrombopoietin or phorbol 12-myrist

275 ine production when Th2 central memory cells are stimulated with thymic stromal lymphopoietin (TSLP)-

276 Peripheral whole-blood samples were stimulated with TLR ligands and analyzed by means o

277 duals with T1D and diabetes-free individuals were stimulated with TLR ligands in the presence and/or

278 IECs were stimulated with TLR ligands, and expression of Fas

279 Fresh PBMCs or CD14(+) monocytes were stimulated with TLR4, TLR7/8-selective ligands, or

280 lpha/beta receptor 1 (IFNAR1)-deficient mice were stimulated with TLR9 or TLR2 ligands.

281 as overcome for SLE-IgG when the endothelium was stimulated with TNF-alpha.

282 rmal human bronchial epithelial (NHBE) cells were stimulated with TNF, IL-4, IFN-gamma, IL-17A, and d

283 issues of patients with RA or osteoarthritis were stimulated with TNFalpha and assayed for gene expre

284 Human aortic EC were stimulated with TNFalpha and treated with TGRL, iso

285 (DEHP) and butyl benzyl phthalate (BBP), and were stimulated with Toll-like receptor (TLR)-9 agonist

286 ment epithelial cells (ARPE-19 and B6-RPE07) were stimulated with toll-like receptor ligands, and ene

287 However, when axons were stimulated with trains of pulses mimicking bursting

288 lood-and peripheral blood-derived mast cells were stimulated with TSLP in vitro to assess PGD2 genera

289 ry (PA) endothelial cells deficient in BMPR2 were stimulated with tumor necrosis factor (TNF), a twof

290 When cells were stimulated with tumor necrosis factor-alpha (or hig

291 When cells were stimulated with tumor promoters, such as epidermal

292 secutive responses when the olfactory neuron is stimulated with two brief pulses.

293 use macrophages and dendritic cells that had been stimulated with type A F. tularensis did not releas

294 Blood was stimulated with ultrapure LPS from Escherichia coli,

295 A mouse macrophage cell line (RAW 264.7) was stimulated with various concentrations of MAX and li

296 nocytes and monocyte-derived dendritic cells were stimulated with various activating ligands, includi

297 o obtain hepatocyte organoid cultures, which were stimulated with various growth factors (GFs) includ

298 om 43 persistent carriers and 49 noncarriers was stimulated with viable S. aureus T-helper type 1 (Th

299 y purified CD28(-) CD45RA(hi) CD8(+) T cells are stimulated with viral peptide presented by autologou

300 Cells were stimulated with voltage pulses; at 1 and 5 Hz frequ